XRCC4 Antilichaam

The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V (D) J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED) . Alternative splicing generates several transcript variants.

7518

Q13426

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-336 of human XRCC4 (NP_071801.1) .

Unconjugated

Primary Antibodies

Apoptosis, Cell Cycle

Affinity purification

Jurkat

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 55kDa

IgG

XRCC4

MCF7

K562

HeLa

Mouse thymus

Mouse heart

DNA repair protein XRCC4

Homo sapiens

DNA repair protein XRCC4, X-ray repair cross-complementing protein 4, XRCC4

WB, IHC, IF

Liquid